510(k) Report

510(k) · Cleared

Cleared

Luminelle DTx Hysteroscopy System

K181909510(k) TraditionalCleared Aug 16, 201830-day reviewClass II21 CFR 876.1500

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Uvision360, Inc. · FAJ Cystoscope And Accessories, Flexible/Rigid

Cleared on Aug 16, 2018 as substantially equivalent to K072180 (Vision-Sciences, Inc., 2007) and 1 other predicate after a 30-day review. Its family tree reaches back 8 generations to 1992. 3 later devices descend from it.

Decided
Aug 16, 2018
Review
30 days
Class
Class II
Product code
FAJ
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K921244 (1992). 19 ancestors in all, the oldest K843084 (1985). 3 later devices descend from it, 1 citing it directly.

  1. Root · 8 generations backK921244 Disposable Protective SheathVision-Sciences, Inc. · 1992
  2. 7 generations backK961591 Disposable Endosheath for E-F100 Flexible NasopharyngoscopeVision-Sciences, Inc. · 1996
  3. 6 generations backK963795 Vision-Sciences Model B-F100 Bronchoscope with Model BS-F21…Vision-Sciences, Inc. · 1996
  4. 5 generations backK021344 B-F200 Bronchoscope with BSS-F21 Endosheath SystemVision-Sciences, Inc. · 2002
  5. 4 generations backK031786 Tne-2000 Esophagoscope with Ecs-D Endosheath SystemVision-Sciences, Inc. · 2003
  6. 3 generations backK040215 Vision-Sciences CST-2000 Flexible Cystoscope with Slide-on…Vision-Sciences, Inc. · 2004
  7. 2 generations backK053560 Modified Endosheath System for Vsi Flexible CystoscopeVision-Sciences, Inc. · 2006
  8. 1 generation backK071127 Flexible Hysteroscope with Endosheath SystemVision-Sciences, Inc. · 2007
  9. This deviceK181909 Luminelle DTx Hysteroscopy SystemUvision360, Inc. · 2018
  10. Descendant · cites it directly · 2 of its ownK190827 Luminelle DTx Hysteroscopy System, Luminelle 360 Rotatable Sterile…Uvision360, Inc. · 2019
  11. Descendant · 2 generations on · 1 of its ownK192278 Luminelle DTx Hysteroscopy System, Luminelle Dx 360 Rotatable…Uvision360, Inc. · 2019
  12. Descendant · 3 generations on · 0 of its ownK210512 LUMINELLE DTx SystemUvision360, Inc. · 2021

Most influential descendants

Showing 3 of 3 · See all
  • K190827Luminelle DTx Hysteroscopy System, Luminelle 360 Rotatable Sterile Disposable Sheath RigidUvision360, Inc. · 2019 · cites it directly2descendants
  • K192278Luminelle DTx Hysteroscopy System, Luminelle Dx 360 Rotatable Disposable Sheath…Uvision360, Inc. · 2019 · 2 generations on1descendant
  • K210512LUMINELLE DTx SystemUvision360, Inc. · 2021 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K921244Disposable Protective SheathVision-Sciences, Inc.1992—
−7K961591Disposable Endosheath for E-F100 Flexible NasopharyngoscopeVision-Sciences, Inc.1996—
−6K963795Vision-Sciences Model B-F100 Bronchoscope with Model BS-F21 Disposable…Vision-Sciences, Inc.1996—
−5K021344B-F200 Bronchoscope with BSS-F21 Endosheath SystemVision-Sciences, Inc.2002—
−4K031786Tne-2000 Esophagoscope with Ecs-D Endosheath SystemVision-Sciences, Inc.2003—
−3K040215Vision-Sciences CST-2000 Flexible Cystoscope with Slide-on Endosheath SystemVision-Sciences, Inc.2004—
−2K053560Modified Endosheath System for Vsi Flexible CystoscopeVision-Sciences, Inc.2006—
−1K071127Flexible Hysteroscope with Endosheath SystemVision-Sciences, Inc.2007—
0 (this device)K181909Luminelle DTx Hysteroscopy SystemUvision360, Inc.2018—
+1K190827Luminelle DTx Hysteroscopy System, Luminelle 360 Rotatable Sterile Disposable…Uvision360, Inc.2019—
+2K192278Luminelle DTx Hysteroscopy System, Luminelle Dx 360 Rotatable Disposable…Uvision360, Inc.2019—
+3K210512LUMINELLE DTx SystemUvision360, Inc.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198510
198910
199220
199320
199410
199610
199910
200210
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201920
202110
FIG. 1 — Lineage of K181909, 1992–2021Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in FAJ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new FAJ device

  1. #1 K193095 Ambu aScope 4 Cystoscore 31.5 · 9 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K072180Vision-Sciences CST-5000 Video Cystoscope with Endosheath System
Summary page 4
…essories Class: II Product Code: FAJ, HIH Predicate Device(s): Primary K072180 Cogentix Flexible Video Cystoscope Predicate with Digital Video Processor and Disposable…
Vision-Sciences, Inc.2007—
*K071127Flexible Hysteroscope with Endosheath System
Summary page 4
…with Digital Video Processor and Disposable EndoSheath Systems Secondary K071127 Vision-Sciences Flexible Cystoscope Predicate with EndoSheath System (with additional…
Vision-Sciences, Inc.2007—

Also cleared against K072180: 2 other devices →

What descends from it? (3)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K190827Luminelle DTx Hysteroscopy System, Luminelle 360 Rotatable Sterile Disposable Sheath RigidUvision360, Inc.20192

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 26 years and passes through 2 companies; a new generation was cleared every 1.9 years on median.
  • 3 of the 19 ancestors have a recall of any class.
  • Of its descendants, K190827 (Uvision360, Inc., 2019) has gone furthest, with 2 descendants of its own.
  • 2 other devices also cite its predicate K072180.

How does its category compare?

All FAJ devices

FAJ Cystoscope And Accessories, Flexible/Rigid: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · FAJ

8in 2025

2007: 22009: 22010: 12012: 12014: 12016: 12017: 22018: 22019: 32020: 22021: 32022: 52023: 52024: 92025: 82026 (partial year): 5
2007high 9 (2024) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FAJ

98in 2025

2019: 207 days median2021: 127 days median2022: 170 days median2023: 207 days median2024: 130 days median2025: 98 days median2026 (partial year): 123 days median
2007high 207 (2019) · low 98 (2025)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · FAJ

7in 2023

2017: 12022: 12023: 7
2007high 7 (2023) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · FAJ

2,690in 2025

2007: 92008: 102009: 102010: 92011: 132012: 82013: 122014: 62015: 282016: 752017: 792018: 792019: 1022020: 3392021: 4942022: 7442023: 9202024: 8922025: 2,690
2007high 2,690 (2025) · low 6 (2014)2025

MAUDE reports naming product code FAJ, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20072—09
20080—010
20092—010
20101—09
20110—013
20121—08
20130—012
20141—06
20150—028
20161—075
20172—179
20182—079
201932070102
20202—0339
202131270494
202251701744
202352077920
202491300892
202589802,690
202651230—

What is it indicated for?

Hysteroscopy: The Luminelle DTx Hysteroscopy System is used to permit direct viewing of the cervical canal and uterine cavity for the purpose of performing diagnostic and surgical procedures. Note: Hysteroscopes are used as tools to access the uterine cavity and are not, in and of themselves, a method of surgery. Generally recognized indications for diagnostic hysteroscopy include: • Abnormal bleeding • Infertility and pregnancy wastage • Evaluation of…

Read the full statement (149 words)

Hysteroscopy: The Luminelle DTx Hysteroscopy System is used to permit direct viewing of the cervical canal and uterine cavity for the purpose of performing diagnostic and surgical procedures.

Note: Hysteroscopes are used as tools to access the uterine cavity and are not, in and of themselves, a method of surgery.

Generally recognized indications for diagnostic hysteroscopy include:

• Abnormal bleeding

• Infertility and pregnancy wastage

• Evaluation of abnormal hysterosalpingogram

• Intrauterine foreign body

• Amenorrhea

• Pelvic pain

Generally recognized indications for operative hysteroscopy include:

• Directed endometrial biopsy

• Polypectomy

• Submucous myomectomy

• Transection of intrauterine adhesions

• Transection of intrauterine septa

• Endometrial ablation

Cystoscopy: The Luminelle DTx Hysteroscopy System is intended for use in endoscopic access to and examination of the lower urinary tract, including the bladder. When combined with accessory instruments, the System allows the user to perform various diagnostic and therapeutic procedures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K181909: Luminelle DTx Hysteroscopy System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K181909

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026